Madsen M B, Kogelman L J A, Kadarmideen H N, Rasmussen H B
Institute of Biological Psychiatry, Mental Health Centre Sct. Hans, Capital Region of Denmark, Roskilde, Denmark.
iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Denmark.
Pharmacogenomics J. 2018 Jan;18(1):144-152. doi: 10.1038/tpj.2016.68. Epub 2016 Oct 18.
Selective serotonin reuptake inhibitors (SSRIs) are the most widely used antidepressants, but the efficacy of the treatment varies significantly among individuals. It is believed that complex genetic mechanisms play a part in this variation. We have used a network based approach to unravel the involved genetic components. Moreover, we investigated the potential difference in the genetic interaction networks underlying SSRI treatment response over time. We found four hub genes (ASCC3, PPARGC1B, SCHIP1 and TMTC2) with different connectivity in the initial SSRI treatment period (baseline to week 4) compared with the subsequent period (4-8 weeks after initiation), suggesting that different genetic networks are important at different times during SSRI treatment. The strongest interactions in the initial SSRI treatment period involved genes encoding transcriptional factors, and in the subsequent period genes involved in calcium homeostasis. In conclusion, we suggest a difference in genetic interaction networks between initial and subsequent SSRI response.
选择性5-羟色胺再摄取抑制剂(SSRIs)是使用最广泛的抗抑郁药,但治疗效果在个体间差异显著。人们认为复杂的遗传机制在这种差异中起作用。我们采用了一种基于网络的方法来揭示其中涉及的遗传成分。此外,我们研究了随着时间推移,SSRIs治疗反应潜在的遗传相互作用网络差异。我们发现,与后续阶段(开始治疗4 - 8周)相比,在SSRIs治疗初期(基线至第4周)有四个中心基因(ASCC3、PPARGC1B、SCHIP1和TMTC2)具有不同的连接性,这表明在SSRIs治疗的不同阶段,不同的遗传网络发挥着重要作用。在SSRIs治疗初期,最强的相互作用涉及编码转录因子的基因,而在后续阶段则涉及参与钙稳态的基因。总之,我们认为SSRIs治疗初期和后续反应的遗传相互作用网络存在差异。